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用001×7阳离子交换树脂经恒温、浓酸浸泡处理成耐氧化阳离子交换树脂的方法。用于镀铬槽液(铬酐浓度为250g/L)的净化。 相似文献
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马铃薯淀粉经环氧氯丙烷交联并在过硫酸钾引发下与丙稀酸接枝成淀粉基阳离子交换树脂,测得交换容量为8.1毫克当量/克,并可以再生。 相似文献
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为了考察不同离子交换树脂组合对制备对离子水质的影响,采用实验室离子交换法制备去离子水简易装置,制备去离子水。通过化学检测法和物理检测法,测定水质质量。结果表明组合"混和离子交换树脂—混和离子交换树脂-混和离子交换树脂"制备的水质,Cl-、SO42-、Ca2+、Mg2+离子完全除净,电导率为0.987μs·cm-1,制备的水质最好,适合实验室制水使用。 相似文献
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植酸盐系列产品如植酸钠、植酸钾、植酸锌等,是新型的精细化工产品。在日用化工、食品发酵、医药、石化、冶金、电镀等许多领域都有重要用途。 关于植酸盐的制备方法,据报道一般是先制备植酸,然后植酸与碱或碱性氧化物发生中和成盐反应制得,此工艺过程需先制备出纯净的植酸,再进行中的反应,后精制浓 相似文献
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美国Dow Chomical公司发现了有分子量较小的全氟乙烯基醚单体。用这类单体制得的全氟碳共聚物做成氯碱工业用离子交换膜,由于有较低的水合作用,显示出某些独特的电化学性能,预计可与目前已商品化的产品竞争。 相似文献
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《国际聚合物材料杂志》2012,61(8):389-397
Thermoresponsive hydrogels with fixed molar ratio (25 mol%) N-isopropylacrylamide (NIPAM) and different concentration of N-tertiary butylacrylamide (NTBA) and hydroxyethylacrylamide (HEAA) were synthesized and characterized. Differential scanning calorimetry indicated that the amount of the bound water and the bound water to total water ratio increased with increasing the hydrophobic NTBA in the hydrogel. The kinetic study of the swelling of hydrogels showed that all samples followed the non-Fickian type of diffusion. The separation efficiency of hydrogels having higher content of HEAA were found to be up to 90% at 5°C but it decreases upon raising the temperature up to 30°C. 相似文献
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新型磺基甜菜碱的合成与性能 总被引:2,自引:0,他引:2
以壬基酚、环氧氯丙烷、二甲胺及2-羟基-3-氯丙磺酸钠为主要原料合成两性表面活性剂N,N-二甲基-N-(2-羟基-3-对壬基苯氧基)丙铵基(2-羟基)丙磺基甜菜碱。通过正交试验设计优化了中间体壬基酚环氧丙基醚的合成工艺条件,并通过红外光谱对目标产物进行结构表征。采用滴体积法确定了该表面活性剂的临界胶束浓度(cmc)和临界胶束浓度下的表面张力(γcmc),其值分别为9.12×10-4 mol/L和27.87 mN/m。并考察了45 ℃下该表面活性剂的乳化性能。 相似文献
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设计合成了一类新型界面助剂,对该类助剂的性能进行了研究,估算出了界面助剂的性能参数。结果表明,该类界面助剂能量提高Al(OH)3/环氧对脂复合材料的冲击强度及耐热性能,是一类有效的界面助剂。 相似文献
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设计合成了以含有丙二腈基团的菲醌结构为电子受体、三苯胺或N,N-二(4-正丁基苯基)苯胺结构为电子给体的D-A-D型纯有机功能染料(Ⅳ和Ⅴ)。利用紫外-可见吸收光谱、荧光发射光谱、循环伏安曲线及理论计算对该类染料及其前体的光学、电化学性质进行了研究。结果表明,染料Ⅳ和Ⅴ在可见光区域均有较宽的吸收带和发射带,其最大吸收波长分别为581和605 nm,最大发射波长分别为442和472 nm;相对于HOMO能级,丙二腈基团的引入对LUMO能级的影响更大。 相似文献
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《分离科学与技术》2012,47(9):1970-1990
Abstract Polyvinyl alcohol(PVOH) has been chemically modified by crosslinking copolymerization of acrylic acid(AA) and hydroxyethylmethacrylate (HEMA) in aqueous solution of PVOH and finally crosslinking PVOH with glutaraldehyde to produce a full interpenetrating network(IPN) membrane. Accordingly, three such full crosslink IPNs i.e., PVAHI, PVAHII and PVAHIII have been synthesized with different weight ratio of PVOH:Poly (AA-co-HEMA) i.e., 1:0.25 (PVAHI), 1:0.50 (PVAHII) and 1:0.75 (PVAHIII). These IPN membranes have been used for pervaporative separation of MTBE-methanol mixtures. All the PVAH membranes were also characterized with various conventional methods like FTIR, mechanical properties, DSC and TGA. Permeability and methanol selectivity of these membranes were found to increase with increasing amount of copolymer in PVOH matrix. However, among the three membranes, PVAHIII were found to show the highest flux but lower selectivity for methanol while PVAHII membrane showed optimum performance in terms of both flux and selectivity. 相似文献
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以4-羟基苯乙酰胺和六氯环三磷腈为原料合成六(4-氨基苯氧基)环三膦腈;再通过β(3,5-二叔丁基4羟基苯基)丙酰氯与六(4-氨基苯氧基)环三膦腈的酰胺化缩合反应,最终合成了一种具有膦腈环结构和6个受阻酚单元的新型功能复合型枝化大分子抗氧剂六[β-(3,5-二叔丁基-4-羟基苯基)丙酰胺苯基]环三膦腈(HACP)。通过红外吸收光谱与核磁共振谱图对HACP的结构进行了表征。以HACP或抗氧剂1010为抗氧组分成功制备聚丙烯(PP)树脂共混物,并对共混物进行了热稳定性、耐老化性能的研究。结果表明,热失重过程中PP/HACP的失重5 %时的温度(T5 %)最高,为391.9 ℃(空气气氛)和410.0 ℃(N2气氛);同时,纯PP在老化7 d后失去力学性能,而PP/HACP或PP/抗氧剂1010,即使在老化14 d后依旧保持一定的力学性能,其中PP/HACP的拉伸强度由38.8 MPa下降到34.1 MPa,衰减率为11.6 %;PP/抗氧剂1010则以25.1 %的衰减率由38.7 MPa下降到29.0 MPa。 相似文献
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A series of Schiff bases, salicylideneaniline derivatives 1–4, was synthesized under mild conditions and characterized by 1H NMR, HRMS, UV-Vis and fluorescence spectra, and single-crystal X-ray diffraction. In solid and aprotic solvents 1–4 exist mainly as E conformers that possess an intramolecular six-membered-ring hydrogen bond. A weak intramolecular C–H···F hydrogen bond is also observed in fluoro-functionalized Schiff base 4, which generates another S(6) ring motif. The C–H···F hydrogen bond further stabilizes its structure and leads it to form a planar configuration. Compounds 1–3 exhibit solely a long-wavelength proton-transfer tautomer emission, while dipole-functionalized Schiff base 4 shows remarkable dual emission originated from the excited-state intramolecular charge transfer (ESICT) and excited-state intramolecular proton transfer (ESIPT) states. Furthermore, the geometric structures, frontier molecular orbitals (MOs) and the potential energy curves for 1–4 in the ground and the first singlet excited state were fully rationalized by density functional theory (DFT) and time-dependent DFT calculations. 相似文献